Difference between revisions of "Jackson Christopher Benjamin"
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|institution=Universitätsinstitut für klinische Chemie | |institution=Universitätsinstitut für klinische Chemie | ||
Inselspital | Inselspital | ||
|address=INO F, 3010 | |address=INO F, 3010 | ||
|city=Bern | |city=Bern | ||
|country=Switzerland | |country=Switzerland | ||
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{{Labelingperson}} | {{Labelingperson}} | ||
== Participated at == | |||
* [[IOC106 Schroecken]] |
Revision as of 10:43, 5 October 2015
Name | Jackson Christopher, |
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Institution | Universitätsinstitut für klinische Chemie
Inselspital |
Address | INO F, 3010, |
City | Bern |
State/Province | |
Country | Switzerland |
Christopher.Jackson@insel.ch | |
Weblink | |
O2k-Network Lab | CH Bern Nuoffer JM |
Labels:
Publications
Published | Reference | |
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Daura 2021 Neurobiol Dis | 2021 | Daura E, Tegelberg S, Yoshihara M, Jackson C, Simonetti F, Aksentjeff K, Ezer S, Hakala P, Katayama S, Kere J, Lehesjoki AE, Joensuu T (2021) Cystatin B-deficiency triggers ectopic histone H3 tail cleavage during neurogenesis. Neurobiol Dis 156:105418. |
BEC 2020.1 doi10.26124bec2020-0001.v1 | 2020 | Gnaiger E et al ― MitoEAGLE Task Group (2020) Mitochondrial physiology. Bioenerg Commun 2020.1. https://doi.org/10.26124/bec:2020-0001.v1 |
Richter 2019 Life Sci Alliance | 2019 | Richter U, Ng KY, Suomi F, Marttinen P, Turunen T, Jackson C, Suomalainen A, Vihinen H, Jokitalo E, Nyman TA, Isokallio MA, Stewart JB, Mancini C, Brusco A, Seneca S, Lombès A, Taylor RW, Battersby BJ (2019) Mitochondrial stress response triggered by defects in protein synthesis quality control. Life Sci Alliance 2:e201800219. |
Ignatenko 2018 Nat Commun | 2018 | Ignatenko O, Chilov D, Paetau I, de Miguel E, Jackson CB, Capin G, Paetau A, Terzioglu M, Euro L, Suomalainen A (2018) Loss of mtDNA activates astrocytes and leads to spongiotic encephalopathy. Nat Commun 9:70. |
Isohanni 2018 Neurogenetics | 2018 | Isohanni P, Carroll CJ, Jackson CB, Pohjanpelto M, Lönnqvist T, Suomalainen A (2018) Defective mitochondrial ATPase due to rare mtDNA m.8969G>A mutation-causing lactic acidosis, intellectual disability, and poor growth. Neurogenetics 19:49-53. |
Jackson 2014 J Med Genet | 2014 | Jackson CB, Nuoffer JM, Hahn D, Prokisch H, Haberberger B, Gautsch M, Häberli A, Gallati S, Schaller A (2014) Mutations in SDHD lead to autosomal recessive encephalomyopathy and isolated mitochondrial Complex II deficiency. J Med Genet 51:170-5. |